EP0061307B1 - Composition à base de cire et d'organopolysiloxane - Google Patents
Composition à base de cire et d'organopolysiloxane Download PDFInfo
- Publication number
- EP0061307B1 EP0061307B1 EP82301394A EP82301394A EP0061307B1 EP 0061307 B1 EP0061307 B1 EP 0061307B1 EP 82301394 A EP82301394 A EP 82301394A EP 82301394 A EP82301394 A EP 82301394A EP 0061307 B1 EP0061307 B1 EP 0061307B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- component
- denotes
- wax
- group
- organopolysiloxane
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title claims description 28
- 229920001296 polysiloxane Polymers 0.000 title claims description 27
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 239000004215 Carbon black (E152) Substances 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 6
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000008240 homogeneous mixture Substances 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 239000003995 emulsifying agent Substances 0.000 claims description 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 150000002430 hydrocarbons Chemical group 0.000 claims 3
- 239000001993 wax Substances 0.000 description 27
- 239000000314 lubricant Substances 0.000 description 6
- 239000002932 luster Substances 0.000 description 6
- 239000012188 paraffin wax Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 125000001183 hydrocarbyl group Chemical group 0.000 description 5
- 235000019809 paraffin wax Nutrition 0.000 description 5
- 235000019271 petrolatum Nutrition 0.000 description 5
- -1 polyol ether esters Chemical class 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 238000009958 sewing Methods 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 235000013871 bee wax Nutrition 0.000 description 3
- 239000012166 beeswax Substances 0.000 description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 description 3
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000004200 microcrystalline wax Substances 0.000 description 2
- 235000019808 microcrystalline wax Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- KMEHEQFDWWYZIO-UHFFFAOYSA-N triacontyl hexadecanoate Chemical group CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC KMEHEQFDWWYZIO-UHFFFAOYSA-N 0.000 description 2
- 238000009941 weaving Methods 0.000 description 2
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 108010013296 Sericins Proteins 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 239000012164 animal wax Substances 0.000 description 1
- 239000013556 antirust agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000000732 arylene group Chemical group 0.000 description 1
- 229940092738 beeswax Drugs 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000027455 binding Effects 0.000 description 1
- 238000009739 binding Methods 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000006459 hydrosilylation reaction Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000012184 mineral wax Substances 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
- 125000001802 myricyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920006136 organohydrogenpolysiloxane Polymers 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000012186 ozocerite Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000012165 plant wax Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000012177 spermaceti Substances 0.000 description 1
- 229940084106 spermaceti Drugs 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09G—POLISHING COMPOSITIONS; SKI WAXES
- C09G1/00—Polishing compositions
- C09G1/06—Other polishing compositions
- C09G1/08—Other polishing compositions based on wax
- C09G1/10—Other polishing compositions based on wax based on mixtures of wax and natural or synthetic resin
- C09G1/12—Other polishing compositions based on wax based on mixtures of wax and natural or synthetic resin mixtures of wax and silicon-containing polycondensates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/06—Polysiloxanes containing silicon bound to oxygen-containing groups
Definitions
- the present invention relates to a composition comprising a wax and an organopolysiloxane. More specifically, the present invention relates to a composition which has excellent lubricating properties, luster-bestowing properties and water-repellent properties and comprises a homogeneous mixture of a wax and an organopolysiloxane bearing at least one silicon- bonded hydrocarbon ester group.
- Waxes are themselves lubricious and are used as lubricants for machine sewing threads. They have come to be widely used as fluff bindings and as lubricants of warps when weaving textiles, or as polishes for automobiles and furniture, etc. Furthermore, as lubrificants for machine sewing thread or as protecting agents for protecting and polishing the surfaces of automobiles and furniture, mixtures of waxes and dimethylpolysiloxane oils or alkylaralkylpolysiloxane oils have come to be used.
- the present invention offers a wax and organopolysiloxane composition of high compatibility, and which excels in lubricity, luster-bestowing properties, and water repellency, and these characteristics are very durable.
- the present invention relates to a composition
- a composition comprising a homogeneous mixture of (A) from 0.5 to 99.5 parts by weight of a wax and (B) from 0.5 to 99.5 parts by weight of an organopolysiloxane havina the formula- wherein R denote a substituted or unsubstituted monovalent hydrocarbon group, Q denotes a hydrocarbon ester group having the formula -R 1 CO 2 R 2 ,Z denotes an R group ora Qgroup, R 1 denotes a divalent hydrocarbon group, R 2 denotes a saturated monovalent hydrocarbon group having at least 3 carbon atoms, m and n each has an average value of zero or more, the sum of m + n has an average value of from 1 to 2000, there being an average of at least one Q group per molecul of organopolysiloxane B and the total weight of component A plus component B being 100 parts by weight.
- Component A of the compositions of this invention can be any well-known wax.
- Suitable waxes for the purpose of this invention include, but are not limited to, animal waxes such as beeswax, spermaceti, lanolin and ceramic wax; plant waxes such as carnauba wax and candelilla wax; mineral waxes such as ozocerite wax, sericin wax, Montan wax, paraffin wax and microcrystalline wax; and synthetic waxes such as oxides of paraffin wax or their esters, cane sugar - aliphatic acid ester waxes, polyol ether esters, higher alcohols - higher aliphatic acid waxes and chlorinated naphthalenes.
- Component B of the compositions of this invention is an organopolysiloxane having the formula-
- each R denotes, independently, a substituted or an unsubstituted monovalent hydrocabon group.
- unsubstituted R groups include, butare not limited to, alkyl groups such as methyl, ethyl, propyl, octyl, and octadecyl; cycloaliphatic groups such as cyclohexyl; alkenyl groups such as vinyl and allyl; aryl groups such as phenyl and tolyl; and arylalkyl groups such as benzyl, 2-phenylethyl and 2-phenylpropyl.
- substituted R groups include, but are not limited to, the above delineated groups bearing halogen substitution or cyano substitution.
- R be selected from alkyl groups and cycloaliphatic groups, and most preferably from alkyl groups. All R groups do not have to be the same.
- R 1 denotes a divalent hydrocarbon group linking a silicon atom and a -CO z R 3 group.
- suitable R' groups include alkylene groups, which are preferred, such as -CH 2 CH 2 -, -CH 2 CH 2 CH 2 -, -CH 2 CHCH 3 ,-CH 2 CH(CH 3 ) CH 2 -and -(CH2)4-; alkylene arylene groups such as -(CH 2 ) 2 C 6 H 4 -; and arylalkylene groups such as -(CH 2 ) 4 CH 2 CHCH 2 C 6 H 5 .
- R 2 is a saturated hydrocarbon group having three or more carbon atoms.
- R 2 groups include alkyl groups, which are preferred, such as propyl, hexyl, decyl, octadecyl and myricyl; and cycloaliphatic groups such as cyclohexyl.
- Alkyl groups having more than 6 carbon atoms are most preferred for improved compatability between wax and organopolysiloxane.
- m and n denote number each having an average value of zero or more, such as 0, 1, 2, 10, 20, 50 and higher, with the restriction that both m and n cannot be zero simultaneously.
- the sum of m + n must be from 1 to 2000, and preferably from 10 to 1000. When m + n is zero the lubricity and luster properties are poor, and when it exceeds 2000 the compatibility of the organopolysiloxane component with the wax component declines.
- Z denotes an R group or a Q group, hereinabove delineated.
- m has a value of zero, at least one Z must be a Q group because the organopolysiloxane component must contain at least one Q group in the composition of this invention.
- Organopolysiloxanes having the above formula have improved compatibility with waxes; however, a highly preferred organopolysiloxane component B for the compositions of this invention has the formula- where m and n each has an average value of at least one and the sum of m + n has an average value of from 10 to 1000.
- Me denotes the methyl radical and R, R 1 and R 2 are the preferred alkyl groups, alkylene groups and alkyl groups, respectively, denoted above.
- These highly preferred organopolysiloxanes provide particularly excellent luster-bestowing properties, lubricating properties and water-repellency properties to the compositions of this invention when used therein as component B.
- a hydrosilylation catalyst such as chloroplatinic acid.
- compositions of this invention can be prepared by mixing from 0.5 to 99.5 parts by weight of the wax component A and from 0.5 to 99.5 parts by weight of the organopolysiloxane component B with the total weight of A + B being 100 parts by weight.
- the amount of each component ranges from 10 to 90, and most preferably from 20 to 80 parts by weight.
- the present composition is obtained merely by heating and mixing component A and component B above the melting point of the wax.
- a solvent common to both component A and component B should be used.
- components A and B should be mixed with an emulsifying agent, such as ester sulfate salts of higher alcohols, alkylbenzenesulfonate, or polyoxyalkylene adducts of higher aliphatic acids, and the mixture heated above the melting point of the wax, emulsified while adding water slowly, and cooled rapidly.
- an emulsifying agent such as ester sulfate salts of higher alcohols, alkylbenzenesulfonate, or polyoxyalkylene adducts of higher aliphatic acids
- composition of the present invention can be combined in the composition of the present invention according to its uses.
- a lubricant for machine sewing threads small amounts of fluid paraffin and trimethylsiloxy-endblocked dimethylpolysiloxane oil can be used, or antistatic agents of ester phosphate systems may be used with it in small amounts.
- perfumes, solvents, water, abrasives, coloring agents, anti-rust agents, or surfactants may also be added.
- the composition of the present invention is useful as a lubricant for machine threads, a lubrificant for warps when weaving textiles, a protective coating agent to preventing rust, or as a polish for automobiles and furniture.
- OX-1949 wax manufactured by Nippon Seiro K.K. obtained by partially oxidizing paraffin wax (35 parts) and the organopolysiloxane expressed by the following structural formula- and having a viscosity of 400 mm 2 /s- 1 (65 parts) were placed in a beaker, and mixed by a stirrer with four paddles for 60 min while heating to 90° C. After it had been uniformly mixed, it was slowly cooled to room temperature while stirring. This liquid mixture was divided into two equal parts, one of which was placed in a transparent glass bottle and left alone at room temperature for 20 d. Then the storage stability of organopolysiloxane and wax was investigated by looking for separation of the components.
- test panels were arranged beneath an artificial shower connected to a water conduit and showered for a total of 20 h, and the initial luster and water repellency, and their durability, were investigated. The results are shown in Table II.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Silicon Polymers (AREA)
- Lubricants (AREA)
Claims (5)
1. Composition, caractérisée en ce qu'elle comprend un mélange homogène de:
A) de 0,5 à 99,5 parties en poids d'une cire, et
B) de 0,5 à 99,5 parties en poids d'un organopolysiloxane ayant la formule:
dans laquelle R est un groupe hydrocarboné monovalent substitué ou non substitué, Q est un groupe ester d'hydrocarbure ayant la formule -R1CO2R2,Z est un groupe R ou un groupe Q, R1 est un groupe hydrocarboné divalent, R2 est un groupe hydrocarboné monovalent saturé ayant au moins 3 atomes de carbone, m et n ont chacun une valeur moyenne de zéro ou plus, la somme m + n a une valeur moyenne de 1 à 2000, une moyenne d'au moins un groupe Q étant présente par molécule d'organopolysiloxane B) et le poids total de constituant A) et de constituant B) étant de 100 parties en poids.
Z(R2SiO)m(RQSiO)nSiR2Z
dans laquelle R est un groupe hydrocarboné monovalent substitué ou non substitué, Q est un groupe ester d'hydrocarbure ayant la formule -R1CO2R2,Z est un groupe R ou un groupe Q, R1 est un groupe hydrocarboné divalent, R2 est un groupe hydrocarboné monovalent saturé ayant au moins 3 atomes de carbone, m et n ont chacun une valeur moyenne de zéro ou plus, la somme m + n a une valeur moyenne de 1 à 2000, une moyenne d'au moins un groupe Q étant présente par molécule d'organopolysiloxane B) et le poids total de constituant A) et de constituant B) étant de 100 parties en poids.
2. Composition selon la revendication 1, dans laquelle R est un groupe alcoyle, R1 est un groupe alcoylène et R2 est un groupe alcoyle.
3. Composition selon la revendication 2, dans laquelle le constituant B) a la formule:
dans laquelle chaque valeur moyenne de m et de n est d'au moins un, la valeur moyenne de m + n va de 10 à 1000 et Me représente le radical méthyle.
4. Composition selon l'une des revendications 1, 2 ou 3, qui comprend, en outre, un ou plusieurs solvants pour le constituant A) et le constituant B).
5. Composition selon l'une des revendications 1, 2 ou 3, qui comprend, en outre, de l'eau et un ou plusieurs agents émulsifiants.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP39902/81 | 1981-03-19 | ||
| JP56039902A JPS57153097A (en) | 1981-03-19 | 1981-03-19 | Organopolysiloxane composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0061307A1 EP0061307A1 (fr) | 1982-09-29 |
| EP0061307B1 true EP0061307B1 (fr) | 1984-08-22 |
Family
ID=12565884
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP82301394A Expired EP0061307B1 (fr) | 1981-03-19 | 1982-03-18 | Composition à base de cire et d'organopolysiloxane |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4404035A (fr) |
| EP (1) | EP0061307B1 (fr) |
| JP (1) | JPS57153097A (fr) |
| CA (1) | CA1184696A (fr) |
| DE (1) | DE3260598D1 (fr) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0274100A2 (fr) * | 1986-12-22 | 1988-07-13 | Wacker Silicones Corporation | Cire d'organopolysiloxane contenant du soufre et son procédé de préparation |
| EP0372205A2 (fr) * | 1988-12-03 | 1990-06-13 | TAIHO INDUSTRIES Co., LTD. | Agent de glaçage pour voiture |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4609545A (en) * | 1982-11-24 | 1986-09-02 | Schlossman Mitchell L | Compressing aid for compressing powders |
| US4591502A (en) * | 1982-11-24 | 1986-05-27 | Schlossman Mitchell L | Compressing aid for cosmetic powders |
| JPS6155159A (ja) * | 1984-08-25 | 1986-03-19 | Nippon Oil Co Ltd | 塗膜保護用水性組成物 |
| US4828885A (en) * | 1985-06-06 | 1989-05-09 | Edge Line Products, Inc. | Ski wax composition and process of application |
| JPH0657820B2 (ja) * | 1987-03-16 | 1994-08-03 | 石原薬品株式会社 | 窓ガラスにワツクス剤が付着しない車輌のツヤ出し方法 |
| JPH01239164A (ja) * | 1988-03-17 | 1989-09-25 | Kanebo Ltd | 繊維構造物の艶出加工方法 |
| JPH0798919B2 (ja) * | 1988-11-29 | 1995-10-25 | 東レ・ダウコーニング・シリコーン株式会社 | ポリッシュ |
| US4936914A (en) * | 1988-12-20 | 1990-06-26 | S. C. Johnson & Con, Inc. | Film-forming emulsion polish compositions containing copolymeric siloxanes |
| US5112394A (en) * | 1990-06-25 | 1992-05-12 | S.C. Johnson & Son, Inc. | Furniture polish concentrate and formulations |
| US5328696A (en) * | 1991-07-22 | 1994-07-12 | Dow Corning Corporation | Devices using silicone pressure sensitive adhesives containing organic wax |
| US5217758A (en) * | 1992-05-15 | 1993-06-08 | Dow Corning Corporation | Silicone containing automotive vinyl protectant |
| GB2270919B (en) * | 1992-09-26 | 1996-04-24 | Sandoz Ltd | Aqueous wax and silicone dispersions,their production and use |
| US5435839A (en) * | 1992-12-24 | 1995-07-25 | Matsushita Electric Industrial Co., Ltd. | Finishing agents and method of manufacturing the same |
| US5703145A (en) * | 1993-06-30 | 1997-12-30 | Hitachi Koki Co., Ltd. | Hot melt type ink composition for ink jet |
| US5998541A (en) | 1995-06-14 | 1999-12-07 | Matsushita Electric Industrial Co., Ltd. | Finishing agents and method of using the same |
| US5962074A (en) * | 1996-06-05 | 1999-10-05 | 3M Innovative Properties Company | Wax composition and method of use |
| US6159551A (en) * | 1998-02-27 | 2000-12-12 | John Yeiser | Wax and method of wax application |
| US6953500B2 (en) | 2001-09-10 | 2005-10-11 | Lewis Glenn H | Water wax emulsion cleaner and waxer |
| US7094449B2 (en) * | 2002-06-21 | 2006-08-22 | Boler Jr Lewyn B | Device and system for coating a surface and reducing surface irregularities |
| US20050233157A1 (en) * | 2002-06-21 | 2005-10-20 | Boler Lewyn B Jr | Device and system for coating a surface |
| WO2008043512A2 (fr) * | 2006-10-10 | 2008-04-17 | Dow Corning Corporation | Agent régulateur de mousse à base de silicone |
| WO2009085200A2 (fr) | 2007-12-21 | 2009-07-09 | Amgen Inc. | Anticorps anti-amyloïde et utilisations de ceux-ci |
| CN102348765B (zh) | 2009-03-10 | 2015-09-09 | 道康宁东丽株式会社 | 水包油硅氧烷乳液组合物 |
| GB0905502D0 (en) | 2009-03-31 | 2009-05-13 | Dow Corning | Organopolysiloxane emulsions and their production |
| GB0905507D0 (en) | 2009-03-31 | 2009-05-13 | Dow Corning | Organopol Ysiloxane Compositions Containing An Active Material |
| WO2012002571A1 (fr) | 2010-07-02 | 2012-01-05 | 東レ・ダウコーニング株式会社 | Composition d'une émulsion de silicone d'huile dans l'eau |
| PL237798B1 (pl) * | 2017-11-17 | 2021-05-31 | Madonis Spolka Z Ograniczona Odpowiedzialnoscia | Środki do pielęgnacji mebli i podłóg drewnianych |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE553159A (fr) * | 1955-12-05 | |||
| US3813425A (en) * | 1971-03-17 | 1974-05-28 | Gen Electric | Process for producing polysiloxane useful as brake fluids |
| US3890271A (en) * | 1973-02-07 | 1975-06-17 | Dow Corning | Polish ingredient |
| US3836371A (en) * | 1973-02-07 | 1974-09-17 | Dow Corning | Polish ingredient |
| US3960574A (en) * | 1974-05-13 | 1976-06-01 | Dow Corning Corporation | Detergent resistant auto polish |
| GB1521309A (en) * | 1975-12-10 | 1978-08-16 | Goldschmidt Ag Th | Textile fibre dressings containing organosilicon compound |
-
1981
- 1981-03-19 JP JP56039902A patent/JPS57153097A/ja active Granted
-
1982
- 1982-03-15 US US06/358,161 patent/US4404035A/en not_active Expired - Lifetime
- 1982-03-18 DE DE8282301394T patent/DE3260598D1/de not_active Expired
- 1982-03-18 CA CA000398740A patent/CA1184696A/fr not_active Expired
- 1982-03-18 EP EP82301394A patent/EP0061307B1/fr not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0274100A2 (fr) * | 1986-12-22 | 1988-07-13 | Wacker Silicones Corporation | Cire d'organopolysiloxane contenant du soufre et son procédé de préparation |
| EP0274100A3 (fr) * | 1986-12-22 | 1990-09-12 | Wacker Silicones Corporation | Cire d'organopolysiloxane contenant du soufre et son procédé de préparation |
| EP0372205A2 (fr) * | 1988-12-03 | 1990-06-13 | TAIHO INDUSTRIES Co., LTD. | Agent de glaçage pour voiture |
| EP0372205A3 (fr) * | 1988-12-03 | 1992-01-15 | TAIHO INDUSTRIES Co., LTD. | Agent de glaçage pour voiture |
| EP0551935A2 (fr) * | 1988-12-03 | 1993-07-21 | TAIHO INDUSTRIES Co., LTD. | Agent de glaçage pour automobile |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57153097A (en) | 1982-09-21 |
| CA1184696A (fr) | 1985-03-26 |
| US4404035A (en) | 1983-09-13 |
| EP0061307A1 (fr) | 1982-09-29 |
| JPS61871B2 (fr) | 1986-01-11 |
| DE3260598D1 (en) | 1984-09-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0061307B1 (fr) | Composition à base de cire et d'organopolysiloxane | |
| CA1123542A (fr) | Formules de produits de polissage | |
| US5174813A (en) | Polish containing derivatized amine functional organosilicon compounds | |
| US5154759A (en) | Polish containing amine functional siloxane | |
| US3508933A (en) | Automobile polish | |
| DE2404138C3 (de) | Zusatz für Poliermittel | |
| CA1205350A (fr) | Melanges aqueux de silicium a teneur de carboxyle | |
| US5326387A (en) | Surface protectant composition | |
| US4462828A (en) | Polishing agent composition | |
| EP0915119A1 (fr) | Compositions contenant des aminosiloxanes | |
| EP0515044A1 (fr) | Compositions à base de siloxane et leur utilisation pour le traitement de fibres | |
| US3814710A (en) | Polish compositions | |
| NL8503028A (nl) | Organosiloxan-oxyalkyleen-copolymeren. | |
| EP0135471A2 (fr) | Procédé de traitement de matériaux textiles | |
| US5110891A (en) | Amine functional siloxanes | |
| US5036123A (en) | Straight oil composition for fibrous material | |
| US3856533A (en) | Surface polishes based on organopolysiloxanes and wax | |
| JPS61111360A (ja) | シロキサンに結合したｕｖ吸収剤を有する乳化重合シリコーンエマルジョンの製法 | |
| US4087478A (en) | Siloxane copolymers and thread finisher prepared therewith | |
| US2804440A (en) | Organopolysiloxane polishes | |
| US5705592A (en) | Fluorosiloxane-containing care compositions | |
| US4831169A (en) | Organopolysiloxane oils | |
| US3960574A (en) | Detergent resistant auto polish | |
| US3221040A (en) | Copolymeric organosilicon lubricants | |
| JP3909132B2 (ja) | 化粧品用添加剤 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| AK | Designated contracting states |
Designated state(s): DE FR GB IT |
|
| 17P | Request for examination filed |
Effective date: 19830308 |
|
| ITF | It: translation for a ep patent filed |
Owner name: UFFICIO BREVETTI RAPISARDI S.R.L. |
|
| GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
| AK | Designated contracting states |
Designated state(s): DE FR GB IT |
|
| REF | Corresponds to: |
Ref document number: 3260598 Country of ref document: DE Date of ref document: 19840927 |
|
| ET | Fr: translation filed | ||
| PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
| 26N | No opposition filed | ||
| ITTA | It: last paid annual fee | ||
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 19971203 Year of fee payment: 17 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19971204 Year of fee payment: 17 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 19971218 Year of fee payment: 17 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19990318 |
|
| GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 19990318 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19991130 |
|
| REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20000101 |